Latest Medical Services Jobs

Statistics Director, Oncology

This role involves leading statistical strategies for key oncology programs, designing robust clinical trials, and mentoring statisticians. The position emphasizes innovation, regulatory interactions, and cross-functional collaboration to advance the development of new cancer therapies.

GSK Stevenage, United Kingdom

On-site Permanent

Senior Director, Global Health Outcomes, ViiV Healthcare

This role involves leading the global health outcomes function at ViiV Healthcare, focusing on evidence generation to support HIV treatment and prevention medicines. Responsibilities include strategic leadership, team management, and collaboration with various stakeholders to ensure credible and decision-relevant evidence for patient access and value demonstration.

GSK United Kingdom

On-site Permanent

Senior Clinical Trial Case Manager

This role involves leading cross-functional teams in reviewing safety data, mentoring junior staff, and ensuring compliance with GxP guidelines and international regulations. The position also focuses on managing pharmacovigilance procedures, conducting impact assessments of new legislation, and supporting regulatory inspections and audits.

CSL

On-site Permanent

Senior Director, Search & Evaluation Late TA Lead, Immunology

This role involves leading strategic sourcing and evaluation of late-stage external Hematology therapeutic area opportunities, from Phase 2 through marketed drugs. Responsibilities include engaging with Key Opinion Leaders, driving due diligence, and shaping the portfolio through high-impact partnerships.

CSL United States £263,000 – £328,000 pa

Hybrid Permanent

Global Development Lead, Internal Medicine, Sr. Director (MD)

The Global Development Lead (GDL) in Internal Medicine is responsible for leading the clinical development of assigned assets, collaborating with cross-functional teams to design and execute clinical trials, and ensuring regulatory compliance. The role involves strategic planning, regulatory submissions, and engagement with external stakeholders to drive the clinical development program.

Pfizer Manchester, M1 4HD, United Kingdom

On-site Permanent

Head of Research and Development

We’re partnering with a market-leader in the Ophthalmology sector, who are looking to recruit an experienced Head of R&D (Research & Development)!The successful candidate will lead R&D strategy, manage a multidisciplinary team, and work closely with key internal functions to...

Evolve Selection Cambridge, Cambridgeshire, United Kingdom

Remote Permanent

Formulation and Application Specialist

Exciting Opportunity: Formulation & Application SpecialistAre you a hands‑on formulation scientist who enjoys seeing products progress from concept through to manufacture? This organisation is seeking a Formulation & Application Specialist to join its R&D function, playing a key role in...

SRG Halifax, West Yorkshire, HX1 1TH, United Kingdom

On-site Permanent

Development & Regulatory Chemist

This role involves developing and validating analytical methods for APIs, authoring and maintaining ASMFs, and supporting regulatory submissions. The chemist will work closely with cross-functional teams, manage method transfers, and ensure regulatory compliance for pharmaceutical ingredients.

SRG Hitchin, Hertfordshire, SG5 1HP, United Kingdom

On-site Permanent

Pharmaceutical Quality Engineer

The role involves providing quality engineering support across manufacturing, validation, and supply chain operations, ensuring compliance with GMP and GDP standards. Key responsibilities include leading deviation investigations, managing CAPA processes, and collaborating with cross-functional teams to drive continuous improvement in quality systems.

Smart4Sciences Cheshire, United Kingdom

On-site Contract Flexible

Chemical Process Operator

This role involves operating chemical process plant and manufacturing equipment, following batch manufacturing instructions, monitoring chemical reactions, and supporting material handling and packaging activities. The position offers long-term stability and development opportunities within a safety and quality-driven manufacturing environment.

Talent STEM Ltd Stradishall, United Kingdom

On-site Permanent Shift-work

Head of Quality Assurance and Regulatory Affairs

Evolve are partnering with a fast-growing organisation to appoint a Head of Quality Assurance & Regulatory Affairs. This is a strategic leadership role where you will drive quality and regulatory excellence, support global expansion, and work cross-functionally to ensure consistently...

Evolve Selection London, United Kingdom

Global Development Lead, Internal Medicine, Sr. Director (non-MD)

The Global Development Lead (GDL) is responsible for leading the clinical development of assigned assets in Internal Medicine. This involves designing, executing, and interpreting clinical studies, creating development plans, and collaborating with cross-functional teams to ensure regulatory submissions and product approvals globally. The role also includes specialized monitoring, regulatory support, and engaging with external stakeholders to drive strategic insights.

Pfizer United States

On-site Permanent

Medicinal Drug Design Lead, London

Isomorphic Labs is applying frontier AI to help unlock deeper scientific insights, faster breakthroughs, and life-changing medicines with an ambition to solve all disease.The future is coming. A future enabled and enriched by the incredible power of machine learning. A...

Isomorphic Labs London, United Kingdom

Research Scientist (Applied LLMs), London

Isomorphic Labs is applying frontier AI to help unlock deeper scientific insights, faster breakthroughs, and life-changing medicines with an ambition to solve all disease.The future is coming. A future enabled and enriched by the incredible power of machine learning. A...

Isomorphic Labs London, United Kingdom

Automation Engineer - Pharmaceutical

This role involves maintaining and troubleshooting automation and control systems in a pharmaceutical manufacturing environment, ensuring compliance with GMP regulations. You will participate in computerized system validation, support continuous improvement projects, and collaborate with cross-functional teams.

Smart4Sciences West Yorkshire, United Kingdom

On-site Permanent